Human mammary 3D spheroid models uncover the role of filopodia in breaching the basement membrane to facilitate invasion Alain Corinus, Sophie Abélanet, Julia Dubreuil, Zhenyu Zhu, Sabrina Pisano, Christelle Boscagli, Anne-Sophie Gay, Delphine Debayle, Marin Truchi, Kevin Lebrigand, Sandra Lacas-Gervais, Frédéric Brau, Xavier Descombes, Patricia Rousselle, Michel Franco, Frédéric Luton Matrix Biology, 2026 • The basement membrane (BM) directs epithelial tissue architecture and behavior. How tumor cells breach this barrier during invasion remains poorly understood. Using minimalist 3D spheroid models mimicking physiological BM assembly, we reveal a novel infiltration mechanism. Filopodia-like protrusions perforate and widen BM pores. This facilitates cell dissemination through sequential protease-independent and -dependent steps. Basement membranes (BM) are thin, nanoporous sheets of specialized extracellular matrix (ECM) that line epithelial tissues. They are dynamic structures that serve multiple key functions, as evidenced by numerous diseases, including cancer progression, that are associated with their alterations. Our understanding of the BM and its communication with adjoining epithelial cells remains highly fragmented due to the BM’s complex molecular architecture, the lack of molecular tools, limitations in utilizing high-resolution imaging techniques to BMs assembled on tissues, and the difficulty of assessing their functional contributions in vivo . Here, by combining multiple -omics analyses and advanced microscopy methodologies, we characterized the BM from two normal human mammary epithelial cell lines, MCF10 and HMLE, grown as spheroids in 3D matrices. Our findings indicate that the spheroids autonomously assemble a BM exhibiting all the molecular, structural, and biophysical characteristics of physiological BM. Using these minimalist model systems, we provide evidence that collagen IV, laminins, perlecan, and hemidesmosomes all overlap in a shared porous lattice. Next, we demonstrate that the invasion-promoting PSD4 /EFA6B knockout, found in patients with breast cancer, decreases the expression of BM components and their assembly on the spheroid surface. We then show that invasive spheroids develop enlarged pores in the BM via filopodia-like plasma membrane extensions, which further expand in a protease-dependent manner, thereby facilitating the passage of invasive cells.
When proteases reshape barriers: Basement membrane remodelling in development, wound healing and tumour progression Clara Legendre, Guila Dayan, Patricia Rousselle FEBS Journal, 2026 Basement membranes (BMs) are dynamic extracellular matrices whose remodelling controls tissue morphogenesis, regeneration and malignant progression. This review examines how a shared protease‐ and extracellular matrix (ECM)‐based machinery reshapes laminin‐ and collagen IV‐rich BMs during development and wound repair, and how the altered levels, localisation and regulation of these components drive cancer invasion. In development, patterned BM thinning, perforation and stiffening driven by MMPs, MT‐MMPs, ADAMTS proteases and nonproteolytic regulators generate gradients that guide branching, tissue elongation and axis formation. In cutaneous wound healing, many of the same proteases (including MMP‐1, MMP‐9, MT1‐MMP, stromelysins, serine proteases and cathepsins) act in transient, spatially restricted patterns so that keratinocytes remodel a provisional matrix at the wound edge and then rebuild a mature dermal–epidermal BM. By contrast, in carcinomas, invadopodia enriched in MT1‐MMP, MMP‐2, MMP‐9 and related proteases concentrate pericellular proteolysis to perforate BMs, while collagen IV ‘escape tracks’ and laminin‐derived cryptic fragments promote proliferation, survival, epithelial–mesenchymal transition and angiogenesis. Finally, we highlight emerging therapeutic strategies, including isoform‐ and site‐selective protease inhibitors and protease‐responsive or protease‐modulating biomaterials, that seek to locally rebalance this protease‐ECM programme to restore BM integrity in chronic wounds and limit invasive growth in cancer.
Self-assembled peptide RADA16 hydrogel supports wound epithelialization by a laminin-332-dependent binding mechanism Chloé Laigle, Marie Buffier, Emélie Clémens, Sharanya Sankar, Patricia Rousselle Acta Biomaterialia, 2026 Re-epithelialization describes the resurfacing of a skin wound with new epidermis as the first step in restoring its integrity and barrier function. In wounds, re-epithelialization progresses from the surrounding wound edges towards the center, forming a continuum in the regeneration of a differentiated epidermis by adhesion to extracellular matrix proteins. Failure of re-epithelialization is a hallmark of chronic wounds and keeps them in a vicious cycle of infection and uncontrolled inflammation that impairs healing. With the increasing number of all forms of chronic wounds, there is an urgent need to develop appropriate therapeutics. To address the lack of a therapeutic solution specifically targeting this burden, we focused on the self-assembling peptide hydrogel RADA16, whose biocompatibility and therapeutic validation for use in humans as a hemostatic agent make it an attractive candidate. Due to its ability to adopt different stiffness and stability properties depending on the peptide concentration, we investigated its most promising formulation to support epidermal regeneration. Our study shows that RADA16 is a scaffold that permits keratinocyte adhesion, proliferation and migration, enabling wound closure both in vitro and in vivo. We demonstrate an effect based on RADA16-specific binding to the keratinocyte major adhesion protein laminin-332, which is essential for these cellular processes. Our study describes the RADA16 hydrogel as the first synthetic, hydrating, stable and resorbable hydrogel that fosters re-epithelialization of wounds through an endogenous and spontaneous laminin-332 binding mechanism. STATEMENT OF SIGNIFICANCE: The study reports on the characterization of a self-assembling peptide hydrogel (RADA16), already in clinical use for its hemostatic properties, with a view to its use for the reepithelialization of skin wounds. The focus on this indication is important as there is currently no hydrogel with healing-promoting properties in clinical practice. The work is significant as it provides an in-depth investigation of the mechanism by which RADA16 supports wound resurfacing, based on its endogenous and spontaneous interaction with the extracellular matrix protein laminin-332, the major adhesion protein produced by epidermal cells. The combination of basic research for therapeutic development with consideration of a global public health problem are assets that characterize this study.
Bioderived Green Algae Metabolite as a Latent Cross-Linking Agent for Protein-Based Hydrogels with High Potential for Skin Repair Applications Giuseppe Melilli, Patricia Rousselle, Mohamed Mehiri, Nathanael Guigo, Didier Pin, Nicolas Sbirrazzuoli ACS Applied Bio Materials, 2025 Despite advances in wound treatment through tissue engineering, the rapid colonization of biomaterials by host cells remains a crucial step toward complete wound healing. Thanks to their excellent biocompatibility, biodegradability, low antigenicity and cost-effectiveness, cross-linked hydrogels have attracted much attention as a viable solution for wound treatment. In this work, we have developed an inovative cross-linking method for gelatin-based hydrogels inspired by the wound closure mechanism of the green algae Caulerpa taxifolia . Caulerpenyne (CYN), a metabolite extracted from the algae, was used as a latent cross-linking agent for gelatin. The covalent cross-linking process is triggered by an in situ and on-demand deacetylation of the enol acetate functionalities of CYN in oxytoxin 2 (OXY) containing 1,4-dialdehyde, which immediately reacts with the lysine residue in gelatin. The content of ε-amino groups in gelatin was monitored as a function of CYN concentration. Swelling and gel content were analyzed as a function of CYN concentration. Morphology, rheological and biological properties were evaluated by in vitro and in vivo tests. Cell adhesion and viability tests performed with OXY-cross-linked hydrogels and compared with non-cross-linked and genipin-cross-linked gelatin showed excellent performance. Their use in whole skin wounds in pigs showed that CYN-cross-linked hydrogels promoted complete skin regeneration without any cytotoxicity, making them extremely promising matrices in the field of regenerative medicine.
Dermal stiffness governs the topography of the epidermis and the underlying basement membrane in young and old human skin Eva Roig‐Rosello, Guila Dayan, Simone Bovio, Patricia Manissier, Elisabeth Errazuriz, Patricia Rousselle Aging Cell, 2024 The epidermis is a stratified epithelium that forms the outer layer of the skin. It is composed primarily of keratinocytes and is constantly renewed by the proliferation of stem cells and their progeny that undergo terminal differentiation as they leave the basal layer and migrate to the skin surface. Basal keratinocytes rest on a basement membrane composed of an extracellular matrix that controls their fate via integrin‐mediated focal adhesions and hemidesmosomes which are critical elements of the epidermal barrier and promote its regenerative capabilities. The distribution of basal cells with optimal activity provides the basement membrane with its characteristic undulating shape; this configuration disappears with age, leading to epidermal weakness. In this study, we present an in‐depth imaging analysis of basal keratinocyte anchorage in samples of human skin from participants across the age spectrum. Our findings reveal that skin aging is associated with the depletion of hemidesmosomes that provide crucial support for stem cell maintenance; their depletion correlates with the loss of the characteristic basement membrane structure. Atomic force microscopy studies of skin and in vitro experiments revealed that the increase in tissue stiffness observed with aging triggers mechanical signals that alter the basement membrane structure and reduce the extent of basal keratinocyte anchorage, forcing them to differentiate. Genomic analysis revealed that epidermal aging was associated with mechanical induction of the transcription factor Krüppel‐like factor 4. The altered mechanical properties of tissue being a new hallmark of aging, our work opens new avenues for the development of skin rejuvenation strategies.
Designed Ankyrin Repeat Proteins provide insights into the structure and function of CagI and are potent inhibitors of CagA translocation by the Helicobacter pylori type IV secretion system Marine Blanc, Clara Lettl, Jérémy Guérin, Anaïs Vieille, Sven Furler, Sylvie Briand-Schumacher, Birgit Dreier, Célia Bergé, Andreas Plückthun, Sandrine Vadon-Le Goff, Rémi Fronzes, Patricia Rousselle, Wolfgang Fischer, Laurent Terradot Plos Pathogens, 2023 The bacterial human pathogen Helicobacter pylori produces a type IV secretion system (cagT4SS) to inject the oncoprotein CagA into gastric cells. The cagT4SS external pilus mediates attachment of the apparatus to the target cell and the delivery of CagA. While the composition of the pilus is unclear, CagI is present at the surface of the bacterium and required for pilus formation. Here, we have investigated the properties of CagI by an integrative structural biology approach. Using Alpha Fold 2 and Small Angle X-ray scattering, it was found that CagI forms elongated dimers mediated by rod-shape N-terminal domains (CagIN) prolonged by globular C-terminal domains (CagIC). Three Designed Ankyrin Repeat Proteins (DARPins) K2, K5 and K8 selected against CagI interacted with CagIC with subnanomolar affinities. The crystal structures of the CagI:K2 and CagI:K5 complexes were solved and identified the interfaces between the molecules, thereby providing a structural explanation for the difference in affinity between the two binders. Purified CagI and CagIC were found to interact with adenocarcinoma gastric (AGS) cells, induced cell spreading and the interaction was inhibited by K2. The same DARPin inhibited CagA translocation by up to 65% in AGS cells while inhibition levels were 40% and 30% with K8 and K5, respectively. Our study suggests that CagIC plays a key role in cagT4SS-mediated CagA translocation and that DARPins targeting CagI represent potent inhibitors of the cagT4SS, a crucial risk factor for gastric cancer development.
The basement membrane in epidermal polarity, stemness, and regeneration Patricia Rousselle, Chloé Laigle, Gaelle Rousselet American Journal of Physiology Cell Physiology, 2022 The epidermis is a specialized epithelium that constitutes the outermost layer of the skin, and it provides a protective barrier against environmental assaults. Primarily consisting of multilayered keratinocytes, the epidermis is continuously renewed by proliferation of stem cells and the differentiation of their progeny, which undergo terminal differentiation as they leave the basal layer and move upward toward the surface, where they die and slough off. Basal keratinocytes rest on a basement membrane at the dermal-epidermal junction that is composed of specific extracellular matrix proteins organized into interactive and mechanically supportive networks. Firm attachment of basal keratinocytes, and their dynamic regulation via focal adhesions and hemidesmosomes, is essential for maintaining major skin processes, such as self-renewal, barrier function, and resistance to physical and chemical stresses. The adhesive integrin receptors expressed by epidermal cells serve structural, signaling, and mechanosensory roles that are critical for epidermal cell anchorage and tissue homeostasis. More specifically, the basement membrane components play key roles in preserving the stem cell pool, and establishing cell polarity cues enabling asymmetric cell divisions, which result in the transition from a proliferative basal cell layer to suprabasal cells committed to terminal differentiation. Finally, through a well-regulated sequence of synthesis and remodeling, the components of the dermal-epidermal junction play an essential role in regeneration of the epidermis during skin healing. Here too, they provide biological and mechanical signals that are essential to the restoration of barrier function.
Altered Distribution and Expression of Syndecan-1 and -4 as an Additional Hallmark in Psoriasis Eleni Koliakou, Manthou Eleni, Ioanna Koumentakou, Nikolaos Bikiaris, Polyanthi Konstantinidou, Patricia Rousselle, Doxakis Anestakis, Elisabeth Lazaridou, Evangelia Kalloniati, Dimosthenis Miliaras, Anna Michopoulou International Journal of Molecular Sciences, 2022 Syndecans act as independent co-receptors to exert biological activities and their altered function is associated with many pathophysiological conditions. Here, syndecan-1 and -4 were examined in lesional skin of patients with psoriasis. Immunohistochemical staining confirmed altered syndecan-1 distribution and revealed absence of syndecan-4 expression in the epidermis. Fibronectin (FN)—known to influence inflammation and keratinocyte hyperproliferation via α5β1 integrin in psoriasis—was also decreased. Syndecan-1 and -4 expression was analyzed in freshly isolated lesional psoriatic human keratinocytes (PHK) characterized based on their proliferation and differentiation properties. mRNA levels of syndecan-1 were similar between healthy and PHK, while syndecan-4 was significantly decreased. Cell growth and release of the pro-inflammatory Tumor Necrosis Factor-alpha (TNFα) were selectively and significantly induced in PHKs plated on FN. Results from co-culture of healthy keratinocytes and psoriatic fibroblasts led to the speculation that at least one factor released by fibroblasts down-regulate syndecan-1 expression in PHK plated on FN. To assay if biological treatments for psoriasis target keratinocyte proliferation, gelatin-based patches enriched with inteleukin (IL)-17α or TNFα blockers were prepared and tested using a full-thickness healthy epidermal model (Phenion®). Immunohistochemistry analysis showed that both blockers impacted the localisation of syndecan-1 within the refined epidermis. These results provide evidence that syndecans expression are modified in psoriasis, suggesting that they may represent markers of interest in this pathology.
Benefit of coupling heparin to crosslinked collagen I/III scaffolds for human dermal fibroblast subpopulations' tissue growth Anna Michopoulou, Eleni Koliakou, Zoi Terzopoulou, Patricia Rousselle, Artemis Palamidi, Doxakis Anestakis, Polyanthi Konstantinidou, Eva Roig‐Rosello, Euterpi Demiri, Dimitris Bikiaris Journal of Biomedical Materials Research Part A, 2022 Currently, there is a lack of models representing the skin dermal heterogeneity for relevant research and skin engineering applications. This is the first study reporting production of dermal equivalents reproducing features of papillary and reticular dermal compartments. Inspired from our current knowledge on the architecture and composition differences between the papillary and reticular dermis, we evaluated different collagen‐based porous materials to serve as scaffolds for the three‐dimensional expansion of freshly isolated papillary and/or reticular fibroblasts. The scaffolds, composed of either collagen I or collagen I and III mixtures, were prepared by lyophilization. Pore size and hydrolytic stability were controlled by crosslinking with 1‐ethyl‐3‐(3‐dimethyl aminopropyl) carbodiimide (EDC) and N‐hydroxysuccinimide (NHS) or EDC/NHS with covalently bound heparin. The evaluation of the resultant “papillary” and “reticular” dermal equivalents was based on the analysis of characteristic features of each dermal compartment, such as cell density and deposition of newly synthetized extracellular matrix components in histological sections. Crosslinking supported cell growth during dermal tissue formation independent on the fibroblast subpopulation. The presence of collagen III seemed to have some positive but non‐specific effect only on the maintenance of the mechanical strength of the scaffolds during dermal formation. Histological analyses demonstrated a significant and specific effect of heparin on generating dermal equivalents reproducing the respective higher papillary than reticular cell densities and supporting distinct extracellular matrix components deposition (three to five times more carbohydrate material deposited by papillary fibroblasts in all scaffolds containing heparin, while higher collagen production was observed only in the presence of heparin).
Extracellular matrix-based cancer targeting Nikos K. Karamanos, Zoi Piperigkou, Alberto Passi, Martin Götte, Patricia Rousselle, Israel Vlodavsky Trends in Molecular Medicine, 2021
Epidermal physiology Patricia Rousselle, Edgar Gentilhomme, Yves Neveux Agache S Measuring the Skin Non Invasive Investigations Physiology Normal Constants Second Edition, 2017
The SFL activity secreted by metastatic carcinoma cells is related to laminin 5 and mediates cell scattering in an integrin-independent manner Journal of Cell Science, 1999
Peptide compositions and their use for the treatment of skin and mucous membrane wounds and in cosmetic applications P Rousselle, C Laigle, MR Buffier, S Sankar, V Mortureux, MG Rioult US Patent App. 19/337,620 , 2026 2026
Human mammary 3D spheroid models uncover the role of filopodia in breaching the basement membrane to facilitate invasion A Corinus, S Abelanet, J Dubreuil, Z Zhu, S Pisano, C Boscagli, AS Gay, ... Matrix Biology , 2025 2025 Citations: 4
Self-assembled peptide RADA16 hydrogel supports wound epithelialization by a laminin-332-dependent binding mechanism. C Laigle, M Buffier, E Clémens, S Sankar, P Rousselle Acta Biomaterialia 209, 194-210 , 2025 2025 Citations: 2
Self-assembled peptide rada16 hydrogel promotes epithelialization of wounds by a laminin-332-dependent scavenging mechanism C Laigle, M Buffier, E Clémens, S Sankar, P Rousselle Acta Biomaterialia , 2025 2025 Citations: 3
Lipidized LL37-loaded PLGA nanocarriers: Bioengineered peptide delivery systems for enhanced wound healing C De Soricellis, C Laigle, L Spinelli, MC Monti, C Amante, P Russo, ... International Journal of Pharmaceutics 677, 125668 , 2025 2025 Citations: 6
Bioderived Green Algae Metabolite as a Latent Cross-Linking Agent for Protein-Based Hydrogels with High Potential for Skin Repair Applications G Melilli, P Rousselle, M Mehiri, N Guigo, D Pin, N Sbirrazzuoli ACS Applied Bio Materials 8 (3), 2558-2568 , 2025 2025 Citations: 2
Peptides and pharmaceutical and cosmetic compositions containing them P Rousselle US Patent App. 18/693,112 , 2025 2025
3D-HEALING: Proof of concept and optimization of an innovative matrix for skin healing M Buffier, P Rousselle Impulsez vos partenariats , 2024 2024
Characterization of the metabolism profile of skin repair and regeneration. A Pavilla, D Pin, B Perrin, P Rousselle Doctoral school BIOLOGIE MOLÉCULAIRE INTÉGRATIVE ET CELLULAIRE PHD Days , 2024 2024
Contribution of confocal and electron correlative microscopy to the investigation of cell adhesion mechanisms in the skin P Rousselle Journée scientifique de la SFR Santé Lyon Est , 2024 2024
The dynamics of extracellular matrix as a new source of inspiration for innovations in the field of healthy skin aging P Rousselle Cosmetic 360: Let's explore innovations , 2024 2024
Self-assembled peptide hydrogels promote epidermal regeneration and epithelialisation of wounds through an extracellular matrix-dependent mechanism C Laigle, S Sankar, M Buffier, P Rousselle Matrix Biology Europe Meeting 2024 , 2024 2024
Additional Cover E Roig‐Rosello, G Dayan, S Bovio, P Manissier, E Errazuriz, P Rousselle Aging Cell 23 (4), e14180 , 2024 2024
Dermal stiffness governs the topography of the epidermis and the underlying basement membrane in young and old human skin E Roig‐Rosello, G Dayan, S Bovio, P Manissier, E Errazuriz, P Rousselle Aging Cell 23 (4), e14096 , 2024 2024 Citations: 33
Extracellular matrix stiffness shapes the skin dermal-epidermal interface P Rousselle EXTRACELLULAR MATRIX AND PATHOLOGIES: FROM RESEARCH TO INNOVATION , 2023 2023
Extracellular matrix mediated regulation of immunity during wound healing P Rousselle, V Gross, A Chessel, B Ragaru, B Herbage, ... European Tissue Repair Society (ETRS) and the Portuguese Society of Stem … , 2023 2023
Targeting extracellular matrix structural proteins: a strategy to fight skin aging. P Rousselle Corsica Medical Aesthetic Conference , 2023 2023
Interactions between cells and the extracellular matrix P Rousselle Printemps de la cardiologie: Recherche fondamentale et Clinique , 2023 2023
Designed Ankyrin Repeat Proteins provide insights into the structure and function of CagI and are potent inhibitors of CagA translocation by the Helicobacter pylori type IV … M Blanc, C Lettl, J Guérin, A Vieille, S Furler, S Briand-Schumacher, ... PLoS Pathogens 19 (5), e1011368 , 2023 2023 Citations: 8
Construire, renouveler, régénérer l’épiderme: plasticité de la jonction dermo-épidermique P Rousselle Actualités en biologie cutanée-CoBIP 2023. Cours francophone de Biologie de … , 2023 2023
MOST CITED SCHOLAR PUBLICATIONS
Kalinin: an epithelium-specific basement membrane adhesion molecule that is a component of anchoring filaments. P Rousselle, GP Lunstrum, DR Keene, RE Burgeson The Journal of cell biology 114 (3), 567-576 , 1991 1991 Citations: 918
Re-epithelialization of adult skin wounds: Cellular mechanisms and therapeutic strategies P Rousselle, F Braye, G Dayan Advanced Drug Delivery Reviews 146, 344-365 , 2019 2019 Citations: 716
Extracellular matrix contribution to skin wound re-epithelialization P Rousselle, M Montmasson, C Garnier Matrix Biology 75, 12-26 , 2019 2019 Citations: 391
Laminin 5 binds the NC-1 domain of type VII collagen P Rousselle, DR Keene, F Ruggiero, MF Champliaud, M Rest, ... The Journal of cell biology 138 (3), 719-728 , 1997 1997 Citations: 368
Human amnion contains a novel laminin variant, laminin 7, which like laminin 6, covalently associates with laminin 5 to promote stable epithelial-stromal attachment. MF Champliaud, GP Lunstrum, P Rousselle, T Nishiyama, DR Keene, ... The Journal of cell biology 132 (6), 1189-1198 , 1996 1996 Citations: 350
Kalinin is more efficient than laminin in promoting adhesion of primary keratinocytes and some other epithelial cells and has a different requirement for integrin receptors. P Rousselle, M Aumailley The Journal of cell biology 125 (1), 205-214 , 1994 1994 Citations: 308
Laminins of the dermo–epidermal junction M Aumailley, P Rousselle Matrix Biology 18 (1), 19-28 , 1999 1999 Citations: 212
Differential expression of laminin‐5 subunits and integrin receptors in human colorectal neoplasia I Sordat, FT Bosman, G Dorta, P Rousselle, D Aberdam, AL Blum, ... The Journal of Pathology: A Journal of the Pathological Society of Great … , 1998 1998 Citations: 195
Laminin 332 in cancer: When the extracellular matrix turns signals from cell anchorage to cell movement P Rousselle, JY Scoazec Seminars in cancer biology 62, 149-165 , 2020 2020 Citations: 189
The human epidermal basement membrane: a shaped and cell instructive platform that aging slowly alters E Roig-Rosello, P Rousselle Biomolecules 10 (12), 1607 , 2020 2020 Citations: 185
Distribution of laminin and fibronectin isoforms in oral mucosa and oral squamous cell carcinoma H Kosmehl, A Berndt, S Strassburger, L Borsi, P Rousselle, U Mandel, ... British journal of cancer 81 (6), 1071-1079 , 1999 1999 Citations: 184
Keratinocyte migration requires α2β1 integrin-mediated interaction with the laminin 5 γ2 chain F Decline, P Rousselle Journal of cell science 114 (4), 811-823 , 2001 2001 Citations: 181
Cytotoxicity evaluation of antiseptics and antibiotics on cultured human fibroblasts and keratinocytes O Damour, SZ Hua, F Lasne, M Villain, P Rousselle, C Collombel Burns 18 (6), 479-485 , 1992 1992 Citations: 177
Contribution of MT1-MMP and of human laminin-5 γ2 chain degradation to mammary epithelial cell migration C Gilles, M Polette, C Coraux, JM Tournier, G Meneguzzi, C Munaut, ... Journal of cell science 114 (16), 2967-2976 , 2001 2001 Citations: 154
Extracellular matrix-based cancer targeting NK Karamanos, Z Piperigkou, A Passi, M Götte, P Rousselle, I Vlodavsky Trends in molecular medicine 27 (10), 1000-1013 , 2021 2021 Citations: 144
Laminin isoforms and their integrin receptors in glioma cell migration and invasiveness: Evidence for a role of α5-laminin (s) and α3β1 integrin T Kawataki, T Yamane, H Naganuma, P Rousselle, I Andurén, ... Experimental cell research 313 (18), 3819-3831 , 2007 2007 Citations: 142
Diagnostic value of indirect immunofluorescence on sodium chloride-split skin in differential diagnosis of subepidermal autoimmune bullous dermatoses RF Ghohestani, JF Nicolas, P Rousselle, AL Claudy Archives of dermatology 133 (9), 1102-1107 , 1997 1997 Citations: 135
Prevalence and clinical significance of anti–laminin 332 autoantibodies detected by a novel enzyme-linked immunosorbent assay in mucous membrane pemphigoid P Bernard, F Antonicelli, C Bedane, P Joly, C Le Roux-Villet, ... JAMA dermatology 149 (5), 533-540 , 2013 2013 Citations: 130
Substrate-specific modulation of a multisubstrate proteinase: C-terminal processing of fibrillar procollagens is the only BMP-1-dependent activity to be enhanced by PCPE-1 C Moali, B Font, F Ruggiero, D Eichenberger, P Rousselle, V François, ... Journal of Biological Chemistry 280 (25), 24188-24194 , 2005 2005 Citations: 128